Viral Genome-Linked Protein (VPg) Is Essential for Translation Initiation of Rabbit Hemorrhagic Disease Virus (RHDV).

Rabbit hemorrhagic disease virus (RHDV), the causative agent of rabbit hemorrhagic disease, is an important member of the caliciviridae family. Currently, no suitable tissue culture system is available for proliferating RHDV, limiting the study of the pathogenesis of RHDV. In addition, the mechanism...

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Main Authors: Jie Zhu, Binbin Wang, Qiuhong Miao, Yonggui Tan, Chuanfeng Li, Zongyan Chen, Huimin Guo, Guangqing Liu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4657913?pdf=render
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spelling doaj-001c47897b3647dab2038b94324699802020-11-25T01:41:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-011011e014346710.1371/journal.pone.0143467Viral Genome-Linked Protein (VPg) Is Essential for Translation Initiation of Rabbit Hemorrhagic Disease Virus (RHDV).Jie ZhuBinbin WangQiuhong MiaoYonggui TanChuanfeng LiZongyan ChenHuimin GuoGuangqing LiuRabbit hemorrhagic disease virus (RHDV), the causative agent of rabbit hemorrhagic disease, is an important member of the caliciviridae family. Currently, no suitable tissue culture system is available for proliferating RHDV, limiting the study of the pathogenesis of RHDV. In addition, the mechanisms underlying RHDV translation and replication are largely unknown compared with other caliciviridae viruses. The RHDV replicon recently constructed in our laboratory provides an appropriate model to study the pathogenesis of RHDV without in vitro RHDV propagation and culture. Using this RHDV replicon, we demonstrated that the viral genome-linked protein (VPg) is essential for RHDV translation in RK-13 cells for the first time. In addition, we showed that VPg interacts with eukaryotic initiation factor 4E (eIF4E) in vivo and in vitro and that eIF4E silencing inhibits RHDV translation, suggesting the interaction between VPg and eIF4E is involved in RHDV translation. Our results support the hypothesis that VPg serves as a novel cap substitute during the initiation of RHDV translation.http://europepmc.org/articles/PMC4657913?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jie Zhu
Binbin Wang
Qiuhong Miao
Yonggui Tan
Chuanfeng Li
Zongyan Chen
Huimin Guo
Guangqing Liu
spellingShingle Jie Zhu
Binbin Wang
Qiuhong Miao
Yonggui Tan
Chuanfeng Li
Zongyan Chen
Huimin Guo
Guangqing Liu
Viral Genome-Linked Protein (VPg) Is Essential for Translation Initiation of Rabbit Hemorrhagic Disease Virus (RHDV).
PLoS ONE
author_facet Jie Zhu
Binbin Wang
Qiuhong Miao
Yonggui Tan
Chuanfeng Li
Zongyan Chen
Huimin Guo
Guangqing Liu
author_sort Jie Zhu
title Viral Genome-Linked Protein (VPg) Is Essential for Translation Initiation of Rabbit Hemorrhagic Disease Virus (RHDV).
title_short Viral Genome-Linked Protein (VPg) Is Essential for Translation Initiation of Rabbit Hemorrhagic Disease Virus (RHDV).
title_full Viral Genome-Linked Protein (VPg) Is Essential for Translation Initiation of Rabbit Hemorrhagic Disease Virus (RHDV).
title_fullStr Viral Genome-Linked Protein (VPg) Is Essential for Translation Initiation of Rabbit Hemorrhagic Disease Virus (RHDV).
title_full_unstemmed Viral Genome-Linked Protein (VPg) Is Essential for Translation Initiation of Rabbit Hemorrhagic Disease Virus (RHDV).
title_sort viral genome-linked protein (vpg) is essential for translation initiation of rabbit hemorrhagic disease virus (rhdv).
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Rabbit hemorrhagic disease virus (RHDV), the causative agent of rabbit hemorrhagic disease, is an important member of the caliciviridae family. Currently, no suitable tissue culture system is available for proliferating RHDV, limiting the study of the pathogenesis of RHDV. In addition, the mechanisms underlying RHDV translation and replication are largely unknown compared with other caliciviridae viruses. The RHDV replicon recently constructed in our laboratory provides an appropriate model to study the pathogenesis of RHDV without in vitro RHDV propagation and culture. Using this RHDV replicon, we demonstrated that the viral genome-linked protein (VPg) is essential for RHDV translation in RK-13 cells for the first time. In addition, we showed that VPg interacts with eukaryotic initiation factor 4E (eIF4E) in vivo and in vitro and that eIF4E silencing inhibits RHDV translation, suggesting the interaction between VPg and eIF4E is involved in RHDV translation. Our results support the hypothesis that VPg serves as a novel cap substitute during the initiation of RHDV translation.
url http://europepmc.org/articles/PMC4657913?pdf=render
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